gingerol

chemical compound
ChemicalSubstance type_of_chemical_entity Q421081
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gingerol

Summary

gingerol is a type of chemical entity[1]. gingerol has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • gingerol's instance of is recorded as type of chemical entity[3].
  • gingerol's physically interacts with is recorded as Transient receptor potential cation channel, subfamily A, member 1[4].
  • gingerol's canonical SMILES is recorded as CCCCCC(CC(=O)CCC1=CC(=C(C=C1)O)OC)O[5].
  • gingerol's chemical formula is recorded as C₁₇H₂₆O₄[6].
  • gingerol is a type of 5-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)decan-3-one[7].
  • gingerol is part of gingerbread[8].
  • gingerol's Commons category is recorded as Gingerols[9].
  • gingerol's found in taxon is recorded as ginger[10].
  • gingerol's found in taxon is recorded as Aframomum melegueta[11].
  • gingerol's found in taxon is recorded as Carum carvi[12].
  • gingerol's found in taxon is recorded as Cinnamomum[13].
  • gingerol's found in taxon is recorded as Cuminum cyminum[14].
  • gingerol's found in taxon is recorded as Illicium verum[15].
  • gingerol's found in taxon is recorded as Myristica fragrans[16].
  • gingerol's found in taxon is recorded as Piper nigrum[17].
  • gingerol's found in taxon is recorded as clove[18].
  • gingerol's found in taxon is recorded as Zingiber[19].
  • gingerol's found in taxon is recorded as Laurus[20].
  • gingerol's found in taxon is recorded as Physcia mediterranea[21].
  • gingerol's has characteristic is recorded as pungency[22].
  • gingerol's isomeric SMILES is recorded as CCCCCC@@HOC@@HO">[23].
  • gingerol's mass is recorded as {'unit': 'Q483261', 'amount': '+294.183109'}[24].
  • gingerol's median lethal dose is recorded as {'unit': 'Q21091747', 'amount': '+250'}[25].
  • gingerol's median lethal dose is recorded as {'unit': 'Q21091747', 'amount': '+58.1'}[26].
  • gingerol's median lethal dose is recorded as {'unit': 'Q21091747', 'amount': '+25.5'}[27].

Why It Matters

gingerol has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[2] gingerol is known by 17 alternative names across languages and contexts.[28]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Compound Interest. compoundchem.com. Provenance: wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . Studies on the constituents of ginger (Zingiber officinale Roscoe) by GC-MS (author's transl). wikidata.org.
  9. [11] . Termite antifeedant activity in Aframomum melegueta. wikidata.org.
  10. [12] . Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. wikidata.org.
  11. [13] . Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. wikidata.org.
  12. [14] . Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. wikidata.org.
  13. [15] . Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. wikidata.org.
  14. [16] . Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. wikidata.org.
  15. [17] . Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. wikidata.org.
  16. [18] . Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. wikidata.org.
  17. [19] . Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. wikidata.org.
  18. [20] . Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. wikidata.org.
  19. [21] . Phytochemical Investigation of New Algerian Lichen Species: Physcia Mediterranea Nimis. wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . PubChem. Retrieved . wikidata.org.
  23. [25] . Retrieved . wikidata.org.
  24. [26] . Retrieved . wikidata.org.
  25. [27] . Retrieved . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [28] . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). gingerol. Retrieved May 3, 2026, from https://4ort.xyz/entity/gingerol
MLA “gingerol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/gingerol.
BibTeX @misc{4ortxyz_gingerol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{gingerol}}, year = {2026}, url = {https://4ort.xyz/entity/gingerol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): gingerol — https://4ort.xyz/entity/gingerol (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 16d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of (5R)-5-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)decan-3-one
    Instance of type of chemical entity
    Has characteristic pungency
    Part of
    + 10 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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